Home NDC 67751-118 Colgate Great Regular Flavor
Product NDC 67751-118
11-digit product format 677510118
Labeler code 67751
Product ID 67751-118_239658a4-9692-0ca2-e063-6394a90a3baa
Type HUMAN OTC DRUG
Nonproprietary name SODIUM MONOFLUOROPHOSPHATE
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Navajo Manufacturing Company Inc.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-11-05
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength 1 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Colgate Great Regular Flavor
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE 1 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C810JCZ56Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 545626 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67751-118-01 Colgate Great Regular Flavor 1 in 1 BLISTER PACK PASTE, DENTIFRICE 1 2 67751-118-01 Colgate Great Regular Flavor 24 g in 1 TUBE PASTE, DENTIFRICE 24 2 67751-118-02 Colgate Great Regular Flavor 24 g in 1 TUBE PASTE, DENTIFRICE 24 2 67751-118-02 Colgate Great Regular Flavor 1 in 1 BLISTER PACK PASTE, DENTIFRICE 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67751-118 COLGATE GREAT REGULAR FLAVOR (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [NAVAJO MANUFACTURING COMPANY INC.] 2 Current NDC, 4 package rows 20241004_f89bf259-b738-8229-e053-6394a90a0c59.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 9 of 41 · 818 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 67751-118-01 67751011801 1 TUBE in 1 BLISTER PACK (67751-118-01) / 24 g in 1 TUBE 1 tube 2005-11-05 No No Current 67751-118-02 67751011802 1 TUBE in 1 BLISTER PACK (67751-118-02) / 24 g in 1 TUBE 1 tube 2005-11-05 No No Current